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Completed Phase 3 Interventional

Research Study to Look at How Well Semaglutide Works in People Living With Heart Failure, Obesity and Type 2 Diabetes

ClinicalTrials.gov ID: NCT04916470

Public ClinicalTrials.gov record NCT04916470. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 3, 2026, 8:06 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Effect of Semaglutide 2.4 mg Once-weekly on Function and Symptoms in Subjects With Obesity-related Heart Failure With Preserved Ejection Fraction, and Type 2 Diabetes

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study will look at how participants' daily life is affected by their heart failure. The study will also look at the change in participants' body weight. This study will compare the effect of semaglutide (a new medicine) compared to "dummy" medicine on body weight and heart failure symptoms. Participants will either get semaglutide or "dummy" medicine, which treatment participants get is decided by chance. Participants will need to take 1 injection once a week. The study medicine is injected with a thin needle in a skin fold in the stomach area, thigh or upper arm. During the study participants will have talks with the study staff about healthy lifestyle and physical activity. The study will last for about 59 weeks, that is a little more than 1 year. Participants will have 12 clinic visits with the study doctor. * At 6 of the visits participants will have blood samples taken. * At 5 of the visits participants will be asked to fill in a questionnaire * At 4 of the visits participants will have to do a 6-minute walking test * At 3 of the visits participants will have a test to check the heart. * participants will have their eyes checked before or at the start of the study and at the end of the study Women cannot take part if pregnant, breast-feeding or plan to become pregnant during the study period.

Study identification

NCT ID
NCT04916470
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
617 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 15, 2021 (Actual)
Primary completion
Oct 11, 2023 (Actual)
Completion
Oct 11, 2023 (Actual)
Last update posted
Nov 26, 2025

2021 – 2023

United States locations

U.S. sites
54
U.S. states
23
U.S. cities
50
Facility City State ZIP Site status
Eastern Shore Rsrch Inst, LLC Fairhope Alabama 36532 —
Mobile Heart Specialists Mobile Alabama 36608 —
National Heart Institute Cal Beverly Hills California 90211 —
John Muir Physicians Network Concord California 94520 —
Valley Clinical Trials Covina California 91723 —
Keck Medical Center of USC - Outpatient Clinic Los Angeles California 90033 —
Valley Clinical Trials, Inc. Northridge California 91325 —
Lundquist Inst-Biomed Innovtn Torrance California 90502 —
New West Physicians,Inc. Golden Colorado 80401 —
Excel Med Ctr Clinical Trials Boca Raton Florida 33434 —
Bay Area Cardiology Associates, P.A. Brandon Florida 33511 —
Baptist Heart Specialists_Jacksonville Jacksonville Florida 32258 —
CV Res Ctr of S Florida Miami Florida 33173 —
Endeavor Health Clinical Operations-NCH Arlington Heights Illinois 60005 —
Endeavor Health Glenbook Hosp Evanston Illinois 60201 —
Northwestern University_Chicago_0 Evanston Illinois 60208 —
Chicago Medical Research LLC Hazel Crest Illinois 60429 —
Deaconess Specialty Physicians Evansville Indiana 47747 —
Ascension St. Vincent Medical Group Indianapolis Indiana 46260 —
Cardiovascular Rsrch of NW_IN Munster Indiana 46321 —
Cotton-O'Neil Heart Center Topeka Kansas 66606 —
Baptist Health Woodland Elizabethtown Kentucky 42701 —
The Research Group of Lexington LLC Lexington Kentucky 40503 —
Baptist Health Louisville Louisville Kentucky 40207 —
Grace Research, LLC Bossier City Louisiana 71111 —
Heart Clinic of Hammond Hammond Louisiana 70403 —
Clinical Trials of Ame, LLC Monroe Louisiana 71201 —
Grace Research, LLC_Shreveport Shreveport Louisiana 71105 —
Louisiana Heart Center_Slidell Slidell Louisiana 70458 —
Ascension Saint Agnes Heart Ca Baltimore Maryland 21229 —
MedStar Good Samaritan Hosp Baltimore Maryland 21239 —
John Hopkins Hospital Baltimore Maryland 21287 —
Elite Research Center Flint Michigan 48532 —
Mayo Clinic Rochester Minnesota 55905 —
Univ of Mississippi Med Ctr Jackson Mississippi 39216 —
Saint Luke's Hospital of Kansas City Kansas City Missouri 64111 —
St Louis Heart & Vascular, P.C. St Louis Missouri 63136 —
Bryan Heart Lincoln Nebraska 68506 —
CHI Health Clinic Cardiology (CUMC - Bergan Mercy) Omaha Nebraska 68124 —
St Francis Hospital Lindner Research Center Greenvale New York 11548 —
NY Presbyt Hosp-W Cornell Med New York New York 10021 —
Carteret Medical Group Morehead City North Carolina 28557 —
Wake Forest Baptist Health Winston-Salem North Carolina 27157 —
Lindner Center,Christ Hospital Cincinnati Ohio 45219 —
Abington Memorial Hospital Abington Pennsylvania 19001 —
Hospital of University of Pennsylvania Philadelphia Pennsylvania 19104 —
Sanford Health_Sioux Falls Sioux Falls South Dakota 57117 —
Tennessee Center for Clinical Trials Tullahoma Tennessee 37388 —
University of Texas Southwestern Medical Center Dallas Texas 75390 —
Angio Cardiac Care of Texas Houston Texas 77025 —
Cardiology Consultants of Danville Inc. Danville Virginia 24541 —
Virginia Heart Falls Church Virginia 22042 —
Virginia Commonwealth University Richmond Virginia 23298-5058 —
Virginia Commonwealth University Richmond Virginia 23298 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 126 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04916470, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 26, 2025 · Synced Oct 3, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04916470 live on ClinicalTrials.gov.

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